chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	917204	917205	A	G	7	GENIC	homozygous	109623469
19	918187	918188	T	C	29	GENIC	homozygous	109623471
19	918234	918235	A	G	13	GENIC	homozygous	109623473
19	918373	918374	G	A	18	GENIC	homozygous	109623475
19	920310	920311	G	T	19	GENIC	homozygous	109623477
19	921381	921382	T	C	30	GENIC	homozygous	109623479
19	921568	921569	C	T	28	GENIC	homozygous	109623481
19	922120	922121	C	T	22	GENIC	homozygous	109623483
19	924166	924167	A	G	24	GENIC	homozygous	109623485
19	925435	925436	A	T	19	GENIC	homozygous	109623487
19	926389	926390	C	G	34	GENIC	homozygous	109623489
19	930372	930373	A	G	36	GENIC	homozygous	109623491
19	930960	930961	G	A	26	GENIC	homozygous	109623493
19	931381	931382	T	C	18	GENIC	homozygous	109623495
19	931512	931513	G	A	31	GENIC	homozygous	109623497
19	932531	932532	C	T	36	GENIC	homozygous	109623499
19	933488	933489	T	C	23	GENIC	homozygous	109623501
19	933748	933749	A	G	15	GENIC	homozygous	109623503
19	933976	933977	G	A	33	GENIC	homozygous	109623505
19	936334	936335	G	A	21	GENIC	homozygous	109623507
19	937351	937352	A	T	24	GENIC	homozygous	109623509
19	937442	937443	T	C	23	GENIC	homozygous	109623511
19	938960	938961	C	G	23	GENIC	homozygous	109623513
19	936027	936028	C	T	40	GENIC	homozygous	109833113